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Photoelectrochemical Homocoupling of Methane under Blue Light Irradiation AITranslate

The University of Kitakyushu; The University of Kitakyushu; The University of Kitakyushu; The University of Kitakyushu; Kyushu Institute of Technology; Doshisha University
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Publisher: ACS
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Abstract AITranslate

Direct conversion of methane (CH4) into valuable chemicals with low-energy input is an important goal in the sustainable chemical industry. Herein, we report a photoelectrochemical activation of CH4 in the gas phase under visible light irradiation at room temperature. The proof-of-concept study revealed that homocoupling of CH4 to form ethane (C2H6) with high selectivity of 54% was induced by photogenerated holes over a tungsten trioxide (WO3) gas-diffusion photoanode coated with a proton-conducting ionomer in the presence of water vapor. The gas–electrolyte–solid triple-phase boundary enables the oxidation of the inert carbon–hydrogen bond of CH4, and the formation of carbon oxides and ethane with a carbon–carbon bond. The gas-phase photoelectrochemical system shows incident photon-to-current conversion efficiency of 11% under blue light at an applied voltage of 1.2 V. This work is also the first demonstration of a visible-light-driven hydrogen evolution from CH4. The hydrogen is separated from CH4 and oxidized products by a solid polymer electrolyte membrane.

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DOI:https://doi.org/10.1021/acsenergylett.8b02436

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Citation Information:

Direct conversion of methane (CH4) into valuable chemicals with low-energy input is an important goal in the sustainable chemical industry. Herein, we report a photoelectrochemical activation of CH4 in the gas phase under visible light irradiation at room temperature. The proof-of-concept study revealed that homocoupling of CH4 to form ethane (C2H6) with high selectivity of 54% was induced by photogenerated holes over a tungsten trioxide (WO3) gas-diffusion photoanode coated with a proton-conducting ionomer in the presence of water vapor. The gas–electrolyte–solid triple-phase boundary enables the oxidation of the inert carbon–hydrogen bond of CH4, and the formation of carbon oxides and ethane with a carbon–carbon bond. The gas-phase photoelectrochemical system shows incident photon-to-current conversion efficiency of 11% under blue light at an applied voltage of 1.2 V. This work is also the first demonstration of a visible-light-driven hydrogen evolution from CH4. The hydrogen is separated from CH4 and oxidized products by a solid polymer electrolyte membrane.

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GB/T 7714-2015 [1] Fumiaki Amano, Ayami Shintani, Kenyou Tsurui, et al. ACS Energy Letters, 2019(4). DOI:10.1021/acsenergylett.8b02436.
MLA [1] Fumiaki Amano, et al., ACS Energy Letters, no. 4, 2019, https://doi.org/10.1021/acsenergylett.8b02436.
APA [1] Fumiaki Amano, Ayami Shintani, Kenyou Tsurui, Hyosuke Mukohara, Teruhisa Ohno, & Sakae Takenaka. (2019). ACS Energy Letters(4). https://doi.org/10.1021/acsenergylett.8b02436
IEEE [1] Fumiaki Amano, Ayami Shintani, Kenyou Tsurui, Hyosuke Mukohara, Teruhisa Ohno, and Sakae Takenaka, ACS Energy Letters, no. 4, 2019, doi: 10.1021/acsenergylett.8b02436.